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用于生物传感应用的透明载酶二氧化硅薄膜的中孔尺寸控制及可加工性

Controlling mesopore size and processability of transparent enzyme-loaded silica films for biosensing applications.

作者信息

Pérez-Anguiano Oswaldo, Wenger Bernard, Pugin Raphaël, Hofmann Heinrich, Scolan Emmanuel

机构信息

Swiss Center for Electronics and Microtechnology (CSEM) , Jaquet-Droz 1, CH-2000 Neuchâtel, Switzerland.

出版信息

ACS Appl Mater Interfaces. 2015 Feb 4;7(4):2960-71. doi: 10.1021/am508630c. Epub 2015 Jan 21.

Abstract

Silica-based nanoporous thin films including large mesopores are relevant as enzyme supports for applications in biosensing. The diffusion and immobilization of large biomolecules such as enzymes in such porous films require the presence of large mesopores. Creating such morphologies based on a bottom-up synthesis using colloidal templates is a challenge in view of the combination of desired material properties and the robustness of the casting process for the fabrication of thin films. Here a strategy to reproducibly synthesize transparent porous silica thin films with submicrometer thickness and homogeneously distributed porosity is presented. For this purpose, polystyrene-poly-2-vinylpyridine (PS-P2VP) amphiphilic block copolymers are used as porogenic templates. Low-chain alcohols are employed as both selective solvents for the P2VP blocks and reaction media for silica synthesis. Rheology measurements reveal a strong influence of the block copolymer length on the behavior of PS-P2VP micelles in suspension. The pore distribution and accessibility into the film are controlled by adjusting the silica to block copolymer weight ratio. The solvent choice is shown to control not only the micelle size and the generated pore morphology but also the structural homogeneity of the films. Finally, the suitability of the synthesized films as supports for enzymes is tested using a model enzyme, horseradish peroxidase EC 1.11.1.7. Our approach is innovative, robust, and reproducible and provides a convenient alternative to synthesize large mesopores up to small macropores (20-100 nm) in nanostructured thin films with applications in biosensing and functional coatings.

摘要

包含大介孔的二氧化硅基纳米多孔薄膜作为酶载体在生物传感应用中具有重要意义。诸如酶等大生物分子在这种多孔薄膜中的扩散和固定需要大介孔的存在。鉴于所需材料特性与用于制造薄膜的浇铸工艺的稳健性相结合,基于使用胶体模板的自下而上合成来创建这种形态是一项挑战。本文提出了一种可重复合成具有亚微米厚度且孔隙率均匀分布的透明多孔二氧化硅薄膜的策略。为此,聚苯乙烯 - 聚 - 2 - 乙烯基吡啶(PS - P2VP)两亲性嵌段共聚物用作致孔模板。低链醇既用作P2VP嵌段的选择性溶剂,又用作二氧化硅合成的反应介质。流变学测量揭示了嵌段共聚物长度对悬浮液中PS - P2VP胶束行为的强烈影响。通过调节二氧化硅与嵌段共聚物的重量比来控制薄膜中的孔分布和可及性。结果表明,溶剂的选择不仅控制胶束尺寸和产生的孔形态,还控制薄膜的结构均匀性。最后,使用模型酶辣根过氧化物酶EC 1.11.1.7测试了合成薄膜作为酶载体的适用性。我们的方法具有创新性、稳健性和可重复性,为在生物传感和功能涂层应用的纳米结构薄膜中合成高达小大孔(20 - 100 nm)的大介孔提供了一种便捷的替代方法。

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